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Nanostructured lipid carriers for percutaneous administration of alkaloids isolated from Aconitum sinomontanum

机译:纳米结构脂质载体用于经皮给药从乌头中提取的生物碱

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摘要

BackgroundLipid-based nanosystems have great potential for transdermal drug delivery. In this study, nanostructured lipid carriers (NLCs) for short-acting alkaloids lappacontine (LA) and ranaconitine (RAN) isolated from Aconitum sinomontanum (AAS) at 69.47 and 9.16% (w/w) yields, respectively, were prepared to enhance percutaneous permeation. Optimized NLC formulations were evaluated using uniform design experiments. Microstructure and in vitro/in vivo transdermal delivery characteristics of AAS-loaded NLCs and solid lipid nanoparticles (SLNs) were compared. Cellular uptake of fluorescence-labeled nanoparticles was probed using laser scanning confocal microscopy and fluorescence-activated cell sorting. Nanoparticle integrity during transdermal delivery and effects on the skin surface were also investigated.
机译:背景基于脂质的纳米系统具有透皮给药的巨大潜力。在这项研究中,制备了短效生物碱lappacontine(LA)和ranaconitine(RAN)的纳米结构脂质载体(NLCs),分别以69.47和9.16%(w / w)的收率从刺头草(Aonitum sinomontanum)(AAS)中分离出来,以增强经皮渗透。使用统一的设计实验评估了优化的NLC配方。比较了载有AAS的NLC和固体脂质纳米颗粒(SLN)的微结构和体外/体内透皮递送特性。使用激光扫描共聚焦显微镜和荧光激活细胞分选技术检测荧光标记纳米颗粒的细胞摄取。还研究了透皮递送过程中的纳米颗粒完整性以及对皮肤表面的影响。

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